Configuration

RECOVER (gene adaptation), trained once on a downsampled set

RECOVER (gene adaptation) trained once on a subsample of measured pairs to predict the viability of held-out pairs.

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Evaluations and results

1 evaluation · 12 results. Different protocols are not a single leaderboard.

Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency

Sorted by RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average) (lower is better). The best value in each column is highlighted. Decimals are rounded for display; each value links to the printed value and its source.

Tested configuration	Protocol and dataset	RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average)	RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average)	RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average)
RECOVER (gene adaptation), trained once on a downsampled setEvaluation	Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	2.5 (0.2) (best in column)	1.9 (0.4) (best in column)	3.9 (0.4) (best in column)
RECOVER (gene adaptation), trained once on a downsampled setEvaluation	Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)	3.7 (1.0)	3.0 (0.4)	5.0 (0.7)
RECOVER (gene adaptation), trained once on a downsampled setEvaluation	Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)	5.9 (1.0)	4.7 (0.5)	7.1 (2.8)
RECOVER (gene adaptation), trained once on a downsampled setEvaluation	Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	6.1 (0.2)	5.6 (1.0)	7.9 (2.0)

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Exact evaluated configurations and original reported results
Tested configuration	Protocol and dataset	Finding	Evidence and details
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)	3.7 (1.0) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average) unitless · lower Uncertainty: SE 1.0. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Horlbeck Jurkat (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "RECOVER", column "Horlbeck Jurkat"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)	3.0 (0.4) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average) unitless · lower Uncertainty: SE 0.4. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Horlbeck Jurkat (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "RECOVER", column "Horlbeck Jurkat"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)	5.0 (0.7) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average) unitless · lower Uncertainty: SE 0.7. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Horlbeck Jurkat (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "RECOVER", column "Horlbeck Jurkat"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	6.1 (0.2) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average) unitless · lower Uncertainty: SE 0.2. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Horlbeck K562 (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "RECOVER", column "Horlbeck K562"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	5.6 (1.0) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average) unitless · lower Uncertainty: SE 1.0. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Horlbeck K562 (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "RECOVER", column "Horlbeck K562"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	7.9 (2.0) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average) unitless · lower Uncertainty: SE 2.0. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Horlbeck K562 (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "RECOVER", column "Horlbeck K562"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)	5.9 (1.0) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average) unitless · lower Uncertainty: SE 1.0. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Norman (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "RECOVER", column "Norman"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)	4.7 (0.5) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average) unitless · lower Uncertainty: SE 0.5. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Norman (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "RECOVER", column "Norman"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)	7.1 (2.8) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average) unitless · lower Uncertainty: SE 2.8. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Norman (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "RECOVER", column "Norman"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	2.5 (0.2) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average) unitless · lower Uncertainty: SE 0.2. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Simpson (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "RECOVER", column "Simpson"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	1.9 (0.4) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average) unitless · lower Uncertainty: SE 0.4. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Simpson (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "RECOVER", column "Simpson"
Configuration: RECOVER (gene adaptation), trained once on a downsampled set	Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency Dataset: Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)	3.9 (0.4) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average) unitless · lower Uncertainty: SE 0.4. Caption: error is SE across three cross-fold replicates Coverage: Not reported scored / Not reported eligible	Independent external evaluation · Source checked Methods, coverage and source RECOVER (gene adaptation), trained once on a downsampled set on Simpson (Tables 1 and 6, RMSE at fixed gene frequency) pheno-20261022-qin2025-protocol-downsampling-rmse Aggregation: Not reported Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "RECOVER", column "Simpson"

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Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Original source · Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.

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Technical metadata and extraction receipts

Stable ID: pheno-20261022-qin2025-config-recover-prediction

areas: cells-tissues
contexts: research
method types: supervised_machine_learning
reported name: RECOVER
configuration type: reported_configuration
foundation model eligible: false
version: As run by Qin et al. 2025 (PMLR 267); no release or commit is printed
access reuse: Run by Qin et al. 2025; their code for this comparator is not separately identified
parameters: Bilinear projection of 128-dimensional gene embeddings, trained on gene-Bliss scores and converted back to viability; learning rate 0.1 (Appendix B, F).
source locator: Table 1 and Table 6, row 'RECOVER'; Appendix B
provenance note: Configuration run by Qin et al. 2025 in this comparison.
review: method: source-hash-verification; scope-review; reviewer: claude; reviewer note: Claude (Opus 5.5) review agent, independent of the extraction agent; no human review claimed; date: 2026-10-22; artifact sha256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb; retrieval url: https://raw.githubusercontent.com/mlresearch/v267/main/assets/qin25g/qin25g.pdf; method note: Re-hashed the PDF in the scratchpad (SHA-256 matches the source record). Read the cited sections in the pdftotext layer of the pinned PDF.; note: Fields checked against the cited locator; nothing found that the source does not state.

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